LEVY ARTICULATING RETRACTOR— 510(k) K920471

Substantially Equivalent

Lifeguard Medical Products, Inc.

FDA 510(k) clearance K920471 for LEVY ARTICULATING RETRACTOR, Substantially Equivalent on 1992-06-23. Applicant: Lifeguard Medical Products, Inc..

Clearance details

Applicant: Lifeguard Medical Products, Inc.
Product code: Code GAD
Advisory panel: General, Plastic Surgery
Date received: 1992-01-28
Decision date: 1992-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: River Forest, IL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GAD

product code GAD

Malfunction: 504
Total: 504

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.